Cefalexin sodiumProduct ingredient for Cephalexin

Name
Cefalexin sodium
Drug Entry
Cephalexin

Cephalexin is the first of the first generation cephalosporins.7,8 This antibiotic contains a beta lactam and a dihydrothiazide.7 Cephalexin is used to treat a number of susceptible bacterial infections through inhibition of cell wall synthesis.9,Label Cephalexin was approved by the FDA on 4 January 1971.12

Accession Number
DBSALT000261
Structure
Synonyms
Not Available
UNII
F78YJG0WXK
CAS Number
38932-40-0
Weight
Average: 369.37
Monoisotopic: 369.07592146
Chemical Formula
C16H16N3NaO4S
InChI Key
NZDYPHVJLWMLJI-CYJZLJNKSA-M
InChI
InChI=1S/C16H17N3O4S.Na/c1-8-7-24-15-11(14(21)19(15)12(8)16(22)23)18-13(20)10(17)9-5-3-2-4-6-9;/h2-6,10-11,15H,7,17H2,1H3,(H,18,20)(H,22,23);/q;+1/p-1/t10-,11-,15-;/m1./s1
IUPAC Name
sodium (6R,7R)-7-[(2R)-2-amino-2-phenylacetamido]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
SMILES
[Na+].[H][C@]12SCC(C)=C(N1C(=O)[C@H]2NC(=O)[C@H](N)C1=CC=CC=C1)C([O-])=O
PubChem Compound
23667618
ChemSpider
56688
ChEBI
59390
Predicted Properties
PropertyValueSource
Water Solubility0.386 mg/mLALOGPS
logP0.51ALOGPS
logP-2.1Chemaxon
logS-3ALOGPS
pKa (Strongest Acidic)3.26Chemaxon
pKa (Strongest Basic)7.23Chemaxon
Physiological Charge0Chemaxon
Hydrogen Acceptor Count5Chemaxon
Hydrogen Donor Count2Chemaxon
Polar Surface Area115.56 Å2Chemaxon
Rotatable Bond Count4Chemaxon
Refractivity99.81 m3·mol-1Chemaxon
Polarizability34.41 Å3Chemaxon
Number of Rings3Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon